Canonical Allele Identifier: CA3711538
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs771082220
gnomAD v3: 6-31356251-G-T
gnomAD v4: 6-31356251-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356251G>T , CM000668.2:g.31356251G>T GRCh38
NC_000006.11:g.31324028G>T , CM000668.1:g.31324028G>T GRCh37
NC_000006.10:g.31432007G>T NCBI36
NG_023187.1:g.5962C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2008C>A
ENST00000481849.6:n.2008C>A
ENST00000497377.6:n.2008C>A
ENST00000640094.2:c.535C>A ENSP00000491275.2:p.Gln179Lys
ENST00000696558.1:c.535C>A ENSP00000512716.1:p.Gln179Lys
ENST00000696559.1:c.535C>A ENSP00000512717.1:p.Gln179Lys
ENST00000696560.1:c.535C>A ENSP00000512718.1:p.Gln179Lys
ENST00000696561.1:c.535C>A ENSP00000512719.1:p.Gln179Lys
ENST00000696562.1:c.535C>A ENSP00000512720.1:p.Gln179Lys
ENST00000412585.7:c.535C>A MANE Select ENSP00000399168.2:p.Gln179Lys
ENST00000412585.6:c.535C>A ENSP00000399168.2:p.Gln179Lys
ENST00000434333.1:c.568C>A ENSP00000405931.1:p.Gln190Lys
ENST00000474381.1:n.410C>A
ENST00000498007.1:n.801C>A
NM_005514.6:c.535C>A NP_005505.2:p.Gln179Lys
XM_011514556.1:c.568C>A XP_011512858.1:p.Gln190Lys
XM_011514557.1:c.535C>A XP_011512859.1:p.Gln179Lys
XR_926175.1:n.545C>A
NM_005514.7:c.535C>A NP_005505.2:p.Gln179Lys
NM_005514.8:c.535C>A MANE Select NP_005505.2:p.Gln179Lys